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Quality Supporter

Do you like working with a variety of stakeholders? Do you have a keen eye for quality? Do you get energised by solving problems and ensuring optimisation? Do you have experience with Deviations and Change Requests? Then you might be the Quality Supporter we are looking for in our Quality Support team.

  

About the department

Sourcing Operations (SoOp) is the inbound supply chain unit in Product Supply, and is responsible for purchasing, quality control, distribution and warehousing of the thousands of materials going into the production worldwide. The job is in the Quality Support Team, a team in Inbound Supply Management, a part of SoOp. Inbound Supply Management is responsible for supporting the supply chain across SoOp in becoming more robust, effective and efficient, and to ensure reliable supply of quality products (raw and packaging materials). 

The Quality Support team is based in Bagsværd and is responsible for driving Deviations, Change Requests and for ensuring continuous improvement of processes and systems that support the quality of products sourced by SoOp.

 

The position

In Sourcing Operations, our ambition is to deliver high quality products and services to our global production sites. As a Quality Supporter, you will be responsible for driving Deviations and Change Requests on raw and packaging materials. The Deviations and Change Requests are handled in close collaboration with colleagues in Novo Nordisk and external suppliers. You will interact with a various number of stakeholders e.g. Packaging lines, Quality Assurance (QA), process experts and Supply Managers. You will need to balance different needs and requests, while both ensuring a high quality and timely execution of your tasks. You will also participate in tasks or projects aiming at improving compliance and continuous improvement of our work processes. 

You can look forward to joining a dynamic organisation where you will get a wide range of contacts internally in Novo Nordisk and with suppliers.

 

Qualifications

Ideally, you have an academic degree within a relevant discipline such as Engineering, MSc, or the like combined with 2-3 years of relevant experience working with inbound supply processes, handling quality documentation, deviations, change requests and you are skilled at systematic problem solving. Additionally, you understand the GMP requirement standards of the pharmaceutical industry. Knowledge of Purchasing and Supply Chain Management is an advantage. 

On a personal level, you are structured, pro-active and it is natural for you to work in a dynamic environment with many simultaneous tasks and changing priorities while managing strict deadlines. You are independent and not afraid to take initiatives, and you contribute positively and actively to the team environment. You are persistent in achieving results at the right quality level and you thrive in solving complex tasks and communicating in a constructive way based on your knowledge and understanding of quality.

 

Working at Novo Nordisk

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

 

Contact

For further information, please contact Pia Bech Vince at +45 3079 2171.

 

Deadline

15 June 2019.

 

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.


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330027853Phoenix-056f6eba12019-06-04T00:00:00Quality Supporter

Do you like working with a variety of stakeholders? Do you have a keen eye for quality? Do you get energised by solving problems and ensuring optimisation? Do you have experience with Deviations and Change Requests? Then you might be the Quality Supporter we are looking for in our Quality Support team.

  

About the department

Sourcing Operations (SoOp) is the inbound supply chain unit in Product Supply, and is responsible for purchasing, quality control, distribution and warehousing of the thousands of materials going into the production worldwide. The job is in the Quality Support Team, a team in Inbound Supply Management, a part of SoOp. Inbound Supply Management is responsible for supporting the supply chain across SoOp in becoming more robust, effective and efficient, and to ensure reliable supply of quality products (raw and packaging materials). 

The Quality Support team is based in Bagsværd and is responsible for driving Deviations, Change Requests and for ensuring continuous improvement of processes and systems that support the quality of products sourced by SoOp.

 

The position

In Sourcing Operations, our ambition is to deliver high quality products and services to our global production sites. As a Quality Supporter, you will be responsible for driving Deviations and Change Requests on raw and packaging materials. The Deviations and Change Requests are handled in close collaboration with colleagues in Novo Nordisk and external suppliers. You will interact with a various number of stakeholders e.g. Packaging lines, Quality Assurance (QA), process experts and Supply Managers. You will need to balance different needs and requests, while both ensuring a high quality and timely execution of your tasks. You will also participate in tasks or projects aiming at improving compliance and continuous improvement of our work processes. 

You can look forward to joining a dynamic organisation where you will get a wide range of contacts internally in Novo Nordisk and with suppliers.

 

Qualifications

Ideally, you have an academic degree within a relevant discipline such as Engineering, MSc, or the like combined with 2-3 years of relevant experience working with inbound supply processes, handling quality documentation, deviations, change requests and you are skilled at systematic problem solving. Additionally, you understand the GMP requirement standards of the pharmaceutical industry. Knowledge of Purchasing and Supply Chain Management is an advantage. 

On a personal level, you are structured, pro-active and it is natural for you to work in a dynamic environment with many simultaneous tasks and changing priorities while managing strict deadlines. You are independent and not afraid to take initiatives, and you contribute positively and actively to the team environment. You are persistent in achieving results at the right quality level and you thrive in solving complex tasks and communicating in a constructive way based on your knowledge and understanding of quality.

 

Working at Novo Nordisk

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

 

Contact

For further information, please contact Pia Bech Vince at +45 3079 2171.

 

Deadline

15 June 2019.

 

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

2019-06-16T00:51:13.160 Do you like working with a variety of stakeholders? Do you have a keen eye for quality? Do you get energised by solving problems and ensuring optimisation? Do you have experience with Deviations and Change Requests? Then you might be the Quality Supporter we are looking for in our Quality Support team. About the department Sourcing Operations (SoOp) is the inbound supply chain unit in Product Supply, and is responsible for purchasing, quality control, distribution and warehousing of the thousands of materials going into the production worldwide. The job is in the Quality Support Team, a team in Inbound Supply Management, a part of SoOp. Inbound Supply Management is responsible for supporting the supply chain across SoOp in becoming more robust, effective and efficient, and to ensure reliable supply of quality products (raw and packaging materials). The Quality Support team is based in Bagsværd and is responsible for driving Deviations, Change Requests and for ensuring continuous improvement of processes and systems that support the quality of products sourced by SoOp. The position In Sourcing Operations, our ambition is to deliver high quality products and services to our global production sites. As a Quality Supporter, you will be responsible for driving Deviations and Change Requests on raw and packaging materials. The Deviations and Change Requests are handled in close collaboration with colleagues in Novo Nordisk and external suppliers. You will interact with a various number of stakeholders e.g. Packaging lines, Quality Assurance (QA), process experts and Supply Managers. You will need to balance different needs and requests, while both ensuring a high quality and timely execution of your tasks. You will also participate in tasks or projects aiming at improving compliance and continuous improvement of our work processes. You can look forward to joining a dynamic organisation where you will get a wide range of contacts internally in Novo Nordisk and with suppliers. Qualifications Ideally, you have an academic degree within a relevant discipline such as Engineering, MSc, or the like combined with 2-3 years of relevant experience working with inbound supply processes, handling quality documentation, deviations, change requests and you are skilled at systematic problem solving. Additionally, you understand the GMP requirement standards of the pharmaceutical industry. Knowledge of Purchasing and Supply Chain Management is an advantage. On a personal level, you are structured, pro-active and it is natural for you to work in a dynamic environment with many simultaneous tasks and changing priorities while managing strict deadlines. You are independent and not afraid to take initiatives, and you contribute positively and actively to the team environment. You are persistent in achieving results at the right quality level and you thrive in solving complex tasks and communicating in a constructive way based on your knowledge and understanding of quality. Working at Novo Nordisk At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. Contact For further information, please contact Pia Bech Vince at 45 3079 2171. Deadline 15 June 2019. Millions rely on us To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.11jobnet056f6eba100000000000IDK_OFIR_02DKDanmark228DKK2019-06-15T00:00:000000https://www.novonordisk.com/careers/working-at-novo-nordisk/job-ad-display.11474.en_GB.html0EuropaDanmarkSjælland & øerStorkøbenhavnHerlevEuropaDanmarkSjælland & øerStorkøbenhavnFuresøEuropaDanmarkSjælland & øerStorkøbenhavnGladsaxe3530803NOVO NORDISK A/S11Novo Alle 12880BagsværdDKDanmark0DKDanmarkDKDanmark8Fuldtid46Permanent764246JobNet4992232499223210021-05-20190https://dispatcher.ofir.dk/statistic/register?context=FeedEntrySearchedCount&feedId=dc2beb84&entryId=056f6ebahttps://dispatcher.ofir.dk/statistic/register?context=FeedEntryDisplayCount&feedId=dc2beb84&entryId=056f6ebahttps://dispatcher.ofir.dk/statistic/register?context=JobApplicationInitiatedCount&feedId=dc2beb84&entryId=056f6eba&page=ShowJob&component=SendApplicationButtonhttps://dispatcher.ofir.dk/statistic/register?context=JobApplicationAppliedCount&feedId=dc2beb84&entryId=056f6eba&page=EmailApplyForm&component=SendApplicationButtonhttps://static.matchwork.com/company/logo/DK/ORS/SoMe/Oevrige/1.jpgEr du den nye Kvalitetsmedarbejder i NOVO NORDISK A/S?12007991Dansk3Læse/ tale315218Kvalitetsmedarbejder0Øvrige361844390noreply@ofir.comDKDanmarkDKDanmark330075881Senior Regulatory Professional RA DevicesRobot Join a fast-changing environment where engaged people do their best every day to get Novo Nordisk medicine and devices approved globally. Our people have a unique combination of scientific insight and the ability to navigate many agendas and stakeholders. That makes Regulatory Affairs a truly interesting place to work but also quite challenging. Are you up for that challenge? About the department RA Devices is part of the Regulatory Affairs CMC Device Area. In RA Devices focus is on medical devices, drug device combination products and our primary responsibility is to provide regulatory input to device projects and products globally. This is achieved by developing and implementing regulatory strategies based on current legislation and regulations. We are also responsible for updating or maintaining regulatory files within the defined area of responsibility, including evaluation of the regulatory implications of changes and necessary actions. You will be cooperating closely with a wide range of stakeholders from e.g. Product Supply, Device R D, QA, Medical Science and Marketing. The job As Senior Regulatory Affairs Professional you will be responsible of compiling and submitting files for Novo Nordisk drug device combination projects and products according to the relevant regulatory strategy in collaboration with stakeholders across Novo Nordisk. You will facilitate the approval process by identifying device key issues, interaction with the regulatory authorities and ensuring timely and high-quality answers to authority questions. You will get a unique opportunity to establish a global network working with our affiliates and to enhance your knowledge by participating in a wide range of projects involving highly skilled people all experts within their field. As the area is moving into handling and managing more and more complex projects involving many stakeholders, this position requires independent drive, proactive and innovative mind-set as well as talent for project management. Qualifications You hold a master s degree in Science, Engineering, Pharmacy or other relevant education and you have minimum 5 years of relevant experience working with regulations of medical devices. Knowledge of international legislation and standards, experience from the pharmaceutical industry as well as project management will be an advantage. It is imperative that you are self-driven, have a strategic mind-set and able to make the right regulatory decisions and thus drive the regulatory agenda. With a proactive and innovative approach, you are able to bring valuable input and set the strategic direction for the project(s). Finally, you can communicate complex regulatory topics to many different stakeholders from R D to production and marketing. You are fluent in written and spoken English, have strong communication skills and you bring a can-do attitude. At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. Contact For further information please contact Pernille Skindhøj at 45 3077 7350 or Karen Kristiansen at 45 3075 5796 Deadline Please apply for the position no later than 9. September 2019. Millions rely on us To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

Join a fast-changing environment where engaged people do their best every day to get Novo Nordisk medicine and devices approved globally.

Our people have a unique combination of scientific insight and the ability to navigate many agendas and stakeholders. That makes Regulatory Affairs a truly interesting place to work – but also quite challenging. Are you up for that challenge?

 

About the department
RA Devices is part of the Regulatory Affairs CMC & Device Area. In RA Devices focus is on medical devices, drug/device combination products and our primary responsibility is to provide regulatory input to device projects and products globally. This is achieved by developing and implementing regulatory strategies based on current legislation and regulations. We are also responsible for updating or maintaining regulatory files within the defined area of responsibility, including evaluation of the regulatory implications of changes and necessary actions. You will be cooperating closely with a wide range of stakeholders from e.g. Product Supply, Device R&D, QA, Medical & Science and Marketing.

 

The job

As Senior Regulatory Affairs Professional you will be responsible of compiling and submitting files for Novo Nordisk drug/device combination projects and products according to the relevant regulatory strategy in collaboration with stakeholders across Novo Nordisk. You will facilitate the approval process by identifying device key issues, interaction with the regulatory authorities and ensuring timely and high-quality answers to authority questions. 

You will get a unique opportunity to establish a global network working with our affiliates and to enhance your knowledge by participating in a wide range of projects involving highly skilled people – all experts within their field. 

As the area is moving into handling and managing more and more complex projects involving many stakeholders, this position requires independent drive, proactive and innovative mind-set as well as talent for project management.
 

Qualifications
You hold a master’s degree in Science, Engineering, Pharmacy or other relevant education and you have minimum 5 years of relevant experience working with regulations of medical devices. Knowledge of international legislation and standards, experience from the pharmaceutical industry as well as project management will be an advantage.
 
It is imperative that you are self-driven, have a strategic mind-set and able to make the right regulatory decisions – and thus drive the regulatory agenda. With a proactive and innovative approach, you are able to bring valuable input and set the strategic direction for the project(s). Finally, you can communicate complex regulatory topics to many different stakeholders from R&D to production and marketing.

You are fluent in written and spoken English, have strong communication skills and you bring a can-do attitude.
 
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
 

Contact
For further information please contact Pernille Skindhøj at +45 3077 7350 or Karen Kristiansen at +45 3075 5796

 

Deadline
Please apply for the position no later than 9. September 2019.

 

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

Novo Nordisk A/SSøborg2019-08-20T00:00:002019-09-09T00:00:00
330076582Senior Risk Data Specialist, CopenhagenRobot Would you like to work closely with market risk data and be a driver of the Bank s data quality improvements? We are now looking for a Senior Risk Data Specialist to join the Group Risk Data team in Copenhagen. Group Risk Data is involved in several projects related to regulatory requirements and firmwide simplification efforts for risk data as well as designing and running daily data controls. The team is part of Group Risk Management and Control, which independently controls and monitors all aspects of risk including credit, market, liquidity and operational risk in Nordea. We are passionate about quality and integrity in our deliveries ensuring that Nordea achieves best in class risk management solutions. At Nordea, we re committed to being a partner our customers and society can count on. Compliance and integrity go hand in hand. Joining us means you ll have an impact on how we do banking today and tomorrow. So, bring your ideas, skills and unique background. With us, you ll be in good company with plenty of opportunities to collaborate, grow and make your mark on something bigger. About this opportunity Welcome to the Group Risk Data team. We add value by ensuring the highest level of data quality and processes following agreed data governance standards and regulation. Presenting data quality performance in a professional way, as well as prioritizing issues are going to be a key for success. In your daily work, you will collaborate closely with a variety of specialists from different parts of the Bank and we expect you to be able to work with a group of stakeholders to deliver results. You also need to understand and be able to understand existing procedures and controls in depth, as well as drive improvement efforts. What you ll be doing: Implementing data quality processes Establishing interactive KPI reports and dashboards Working on governance, procedures and documentation of market risk data Running and improving daily market risk data controls You ll join team Group Risk Data team. The role is based in Copenhagen. Who you are Collaboration. Ownership. Passion. Courage. These are the values that guide us in being at our best and that we imagine you share with us. To succeed in this role, we believe that you: Have senior experience in working with financial risk data and can take ownership of tasks driving them from beginning to end Are familiar with a range of financial instruments and have a good understanding of risk models, the basics of valuation of financial derivatives, understand derived market data objects like curves and surfaces as well as knowledge in data architecture and IT systems Are outgoing, communicate effectively and can build good relationships with colleagues with diverse competences, nationalities and job responsibilities. You can make the necessary prioritization calls and focus on the key deliveries Your experience and background: Master s degree in Finance, Economics or a related discipline At least 5 years of experience within financial markets and or financial risk Experience with databases and data models including good command of SQL, as well as experience with financial regulations Additional programming or BI experience is a plus Strong written and spoken skills in English If this sounds like you, get in touch! Next steps Submit your application no later than 31 August 2019. For more information, you re welcome to contact Akos Szilagyi. Phone: 45 55 46 79 74, Email: akos.szilagyi@nordea.com. At Nordea, we know that an inclusive workplace is a sustainable workplace. We deeply believe that our diverse backgrounds, experiences, characteristics and traits make us better at serving customers and communities. So please come as you are.

Would you like to work closely with market risk data and be a driver of the Bank’s data quality improvements? We are now looking for a Senior Risk Data Specialist to join the Group Risk Data team in Copenhagen.     

Group Risk Data is involved in several projects related to regulatory requirements and firmwide simplification efforts for risk data as well as designing and running daily data controls. The team is part of Group Risk Management and Control, which independently controls and monitors all aspects of risk including credit, market, liquidity and operational risk in Nordea. We are passionate about quality and integrity in our deliveries ensuring that Nordea achieves “best in class” risk management solutions.

At Nordea, we’re committed to being a partner our customers and society can count on. Compliance and integrity go hand in hand. Joining us means you’ll have an impact on how we do banking – today and tomorrow. So, bring your ideas, skills and unique background. With us, you’ll be in good company with plenty of opportunities to collaborate, grow and make your mark on something bigger. 

About this opportunity

Welcome to the Group Risk Data team. We add value by ensuring the highest level of data quality and processes following agreed data governance standards and regulation. Presenting data quality performance in a professional way, as well as prioritizing issues are going to be a key for success.

In your daily work, you will collaborate closely with a variety of specialists from different parts of the Bank and we expect you to be able to work with a group of stakeholders to deliver results. You also need to understand and be able to understand existing procedures and controls in depth, as well as drive improvement efforts.

What you’ll be doing:

  • Implementing data quality processes
  • Establishing interactive KPI reports and dashboards
  • Working on governance, procedures and documentation of market risk data
  • Running and improving daily market risk data controls

You’ll join team Group Risk Data team. The role is based in Copenhagen.

Who you are

Collaboration. Ownership. Passion. Courage. These are the values that guide us in being at our best – and that we imagine you share with us. To succeed in this role, we believe that you:

  • Have senior experience in working with financial risk data and can take ownership of tasks driving them from beginning to end
  • Are familiar with a range of financial instruments and have a good understanding of risk models, the basics of valuation of financial derivatives, understand derived market data objects like curves and surfaces as well as knowledge in data architecture and IT systems
  • Are outgoing, communicate effectively and can build good relationships with colleagues with diverse competences, nationalities and job responsibilities. You can make the necessary prioritization calls and focus on the key deliveries

Your experience and background:  

  • Master’s degree in Finance, Economics or a related discipline
  • At least 5 years of experience within financial markets and/or financial risk
  • Experience with databases and data models including good command of SQL, as well as experience with financial regulations
  • Additional programming or BI experience is a plus
  • Strong written and spoken skills in English

If this sounds like you, get in touch!

Next steps

Submit your application no later than 31 August 2019.

For more information, you’re welcome to contact Akos Szilagyi. Phone: +45 55 46 79 74, Email: akos.szilagyi@nordea.com.

At Nordea, we know that an inclusive workplace is a sustainable workplace. We deeply believe that our diverse backgrounds, experiences, characteristics and traits make us better at serving customers and communities. So please come as you are.

NORDEA FINANS DANMARK A/STaastrup2019-08-21T00:00:002019-08-31T00:00:00
330074787ScanPeople søger en QA/QC-koordinator til kraftigt vækstende produktion i BallerupRobot På vegne af vores kunde i Ballerup, søger ScanPeople en dygtig QA QC-koordinator til deres kraftigt vækstende produktion. De beskæftiger ca. 40 medarbejdere i dag, og vil i løbet af 2019 gennemgå stor vækst. Virksomheden fokuserer kontinuerligt på at udvikle og forbedre deres måde at producere på - derfor søges der efter nye og dygtige medarbejdere. Virksomheden er i gang med en kraftig udvidelse af deres produktionsudstyr og arbejdsfaciliteter. Så inden for de næste par år, vil der ske rigtig meget nyt og spændende på den front. DINE ARBEJDSOPGAVER At agere som tovholder i organisationen, samt på kvalitetssikringen og vedligeholdelsen af virksomhedens ISO9001-system. At være ansvarlig for gennemgang og foretagelse af diverse afvigelsesrapporter og QA QC-aktiviteter. At sørge for Batch- og råvare-godkendelser. At stå for håndtering af produkt- og materialecertifikater (internt eksternt). At stå for kalibrering, opmåling og overvågning af udstyr, da dette også er en vigtig del af dagligdagen. At agere som koordinator på henholdsvis leverandør- og interne audits. At styre virksomhedens ramp-up på membranproduktionen. At varetage virksomhedens opbygning af ISO9001-systemet, på fabrikken i Hobro. Der kan derfor forekomme enkelte rejsedage til Hobro. DIN PROFIL Du har en baggrund som kvalitetsansvarlig eller kvalitetstekniker. Du har minimum 2-3 års erfaring fra en tilsvarende stilling. Du kan arbejde selvstændigt, og have mange bolde i luften på samme tid. Du arbejder struktureret, og er omstillingsparat når der er behov for dette. Du er klar til løbende at tilegne dig nye færdigheder, og til at håndtere udfordringer samt forandringer, som ligger foran dig. Du tager ansvar og er yderst bevidst om kvaliteten i dit arbejde. Du kan kommunikere på både dansk og engelsk i skrift og tale, samt behersker IT på brugerniveau. VIRKSOMHEDEN TILBYDER En afvekslende og alsidig hverdag i et uformelt produktionsmiljø. En virksomhed i vækst og med en super spændende fremtid. Fremragende personlige- og faglige udviklingsmuligheder. En lønpakke der modsvarer dine kvalifikationer, samt pensionsordning. En spændende fremtid med vækst og gode oplevelser, sammen med kompetente kollegaer. ANSØGNINGSFRISTVi ønsker at besætte stillingen hurtigst muligt og kalder løbende til samtaler. Vi venter på den rette kandidat, men send hellere din ansøgning i dag end i morgen. ANSØGNING Finder du ovenstående lige så spændende som os og er du klar til nye udfordringer, skal du via nedenstående link indtaste dine oplysninger og uploade ansøgning og CV. Har du nogle spørgsmål til stillingen, kan du kontakte Thomas Rastad eller Oscar Brammer på 43 31 00 71. SØG JOBBET HER http: www.scanpeople.axp.dk index.php?axp_act adetails version 1 axp_recruitment_references[] 11134 OBS: Hvis du allerede har registreret dig via vores database, skal du blot logge ind og tilføje jobkoden 11134 for at søge jobbet. Vi ser frem til at modtage din ansøgning! OM SCANPEOPLEScanPeople er en solid og dynamisk, danskejet virksomhed i Scanavo gruppen. En af ScanPeoples store styrker er medarbejdernes meget forskelligartede baggrunde. Vores succes som servicevirksomhed afhænger af et godt og effektivt samspil mellem os, vores kunder og vores kandidater. Vi besidder et vidtrækkende netværk og suppleret med en god solid teoretisk og praktisk baggrund, sikrer vi den bedste service og kvalitet til alle vi er i berøring med. Vi er yderst servicemindede og kompetente rådgivere med en bred erfaring indenfor vikarassistance, search, rekruttering, interim management og outplacement. Vi har med ScanPeoples blå division specialiseret os i at levere personale indenfor Industri, Medico, Teknik og Pharma. Vi har med ScanPeoples grønne division specialiseret os i at levere personale indenfor Salg, Marketing, Kontor og Administration. Yderligere information findes på: www.scanpeople.dk

På vegne af vores kunde i Ballerup, søger ScanPeople en dygtig QA/QC-koordinator til deres kraftigt vækstende produktion. De beskæftiger ca. 40 medarbejdere i dag, og vil i løbet af 2019 gennemgå stor vækst. Virksomheden fokuserer kontinuerligt på at udvikle og forbedre deres måde at producere på - derfor søges der efter nye og dygtige medarbejdere. Virksomheden er i gang med en kraftig udvidelse af deres produktionsudstyr og arbejdsfaciliteter. Så inden for de næste par år, vil der ske rigtig meget nyt og spændende på den front.

DINE ARBEJDSOPGAVER

  • At agere som tovholder i organisationen, samt på kvalitetssikringen og vedligeholdelsen af virksomhedens ISO9001-system.
  • At være ansvarlig for gennemgang og foretagelse af diverse afvigelsesrapporter og QA/QC-aktiviteter.
  • At sørge for Batch- og råvare-godkendelser.
  • At stå for håndtering af produkt- og materialecertifikater (internt & eksternt).
  • At stå for kalibrering, opmåling og overvågning af udstyr, da dette også er en vigtig del af dagligdagen.
  • At agere som koordinator på henholdsvis leverandør- og interne audits.
  • At styre virksomhedens ramp-up på membranproduktionen.
  • At varetage virksomhedens opbygning af ISO9001-systemet, på fabrikken i Hobro. Der kan derfor forekomme enkelte rejsedage til Hobro.

DIN PROFIL

  • Du har en baggrund som kvalitetsansvarlig eller kvalitetstekniker.
  • Du har minimum 2-3 års erfaring fra en tilsvarende stilling.
  • Du kan arbejde selvstændigt, og have mange bolde i luften på samme tid.
  • Du arbejder struktureret, og er omstillingsparat når der er behov for dette.
  • Du er klar til løbende at tilegne dig nye færdigheder, og til at håndtere udfordringer samt forandringer, som ligger foran dig.
  • Du tager ansvar og er yderst bevidst om kvaliteten i dit arbejde.
  • Du kan kommunikere på både dansk og engelsk i skrift og tale, samt behersker IT på brugerniveau.

VIRKSOMHEDEN TILBYDER

  • En afvekslende og alsidig hverdag i et uformelt produktionsmiljø.
  • En virksomhed i vækst og med en super spændende fremtid.
  • Fremragende personlige- og faglige udviklingsmuligheder.
  • En lønpakke der modsvarer dine kvalifikationer, samt pensionsordning.
  • En spændende fremtid med vækst og gode oplevelser, sammen med kompetente kollegaer.

ANSØGNINGSFRIST
Vi ønsker at besætte stillingen hurtigst muligt og kalder løbende til samtaler. Vi venter på den rette kandidat, men send hellere din ansøgning i dag end i morgen.

ANSØGNING
Finder du ovenstående lige så spændende som os og er du klar til nye udfordringer, skal du via nedenstående link indtaste dine oplysninger og uploade ansøgning og CV.

Har du nogle spørgsmål til stillingen, kan du kontakte Thomas Rastad eller Oscar Brammer på 43 31 00 71.

SØG JOBBET HER
http://www.scanpeople.axp.dk/index.php?axp_act=adetails&version=1&axp_recruitment_references[]=11134   
OBS: Hvis du allerede har registreret dig via vores database, skal du blot logge ind og tilføje jobkoden 11134 for at søge jobbet.

Vi ser frem til at modtage din ansøgning!

OM SCANPEOPLE
ScanPeople er en solid og dynamisk, danskejet virksomhed i Scanavo gruppen. En af ScanPeoples store styrker er medarbejdernes meget forskelligartede baggrunde. Vores succes som servicevirksomhed afhænger af et godt og effektivt samspil mellem os, vores kunder og vores kandidater.

Vi besidder et vidtrækkende netværk og suppleret med en god solid teoretisk og praktisk baggrund, sikrer vi den bedste service og kvalitet til alle vi er i berøring med. Vi er yderst servicemindede og kompetente rådgivere med en bred erfaring indenfor vikarassistance, search, rekruttering, interim management og outplacement.

Vi har med ScanPeoples blå division specialiseret os i at levere personale indenfor Industri, Medico, Teknik og Pharma.

Vi har med ScanPeoples grønne division specialiseret os i at levere personale indenfor Salg, Marketing, Kontor og Administration. Yderligere information findes på: www.scanpeople.dk

SCANPEOPLE ApSBallerup2019-08-19T00:00:002019-08-28T00:00:00
330077559Akademisk medarbejder til DANAKRobot Har du lyst til at arbejde med bedømmelse af akkrediterede laboratorier inden for kalibrering samt fysisk, mekanisk og elektrisk prøvning, og være med til at lægge grundlaget for national og international anerkendelse af laboratorier så er du måske vores nye medarbejder. Som ledende assessor hos DANAK får du en uddannelse, der vil lære dig om de metoder vi bruger til bedømmelse af laboratorier og sikre dig forståelse for de akkrediteringsstandarder, som laboratorierne arbejder i henhold til. I uddannelsesforløbet vil du først være observatør på et antal bedømmelser, hvorefter du under supervision selv skal varetage bedømmelse af et antal laboratorier før du godkendes som ledende assessor. Bedømmelsesarbejdet omfatter udvælgelse og ledelse af et bedømmelseshold, som udover dig består af et antal eksperter (tekniske assessorer), oftest 1-2 men i visse tilfælde op til 4-8 eksperter. Du skal desuden koordinere og planlægge bedømmelsen og varetage afrapporteringen og den opfølgning, som ligger til grund for, at et laboratorium kan akkrediteres. Udover bedømmelse af laboratorier vil du kunne blive inddraget i drift af infrastrukturen i DANAK, som bl.a. omfatter betjening af sektorudvalg, kontakt til myndigheder, deltagelse i internationale arbejdsgrupper og komiteer, afvikling af kurser for de akkrediterede laboratorier samt regelmæssige møder med de tekniske assessorer. Vi kan tilbyde spændende og afvekslende arbejdsopgaver i et dynamisk miljø, med gode kollegaer og en uformel omgangstone. Du kommer til at arbejde i laboratoriesektionen både på vores kontor i Skovlunde og hos de akkrediterede laboratorier i hele landet. Da der er en vis rejseaktivitet knyttet til arbejdet med lange arbejdsdage til følge, vil du have flekstid og gode muligheder for fleksibilitet i at planlægge dit arbejde. Om osDANAK (Den danske Akkrediteringsfond) er en selvstændig og uafhængig fond, og er Danmarks nationale akkrediteringsorgan, som foretager akkreditering af danske virksomheder. DANAKs mission er at sikre troværdig dokumentation for overholdelse af kravspecifikationer gennem akkreditering. Det gør vi ved at akkreditere laboratorier, certificerings- og inspektionsorganer mv. til at kalibrere, måle, certificere og foretage inspektioner efter internationale standarder. Vi har et tæt samarbejde med myndigheder i Danmark og akkrediteringsorganer i andre lande. DANAK har 30 fastansatte medarbejdere, hvoraf 23 er ledende assessorer, samt 130 eksperter tilknyttet. DANAK har akkrediteret ca. 200 laboratorier, 40 certificeringsorganer og 50 inspektionsorganer. Om digVi forestiller os, at du er akademiker eller tilsvarende med en relevant naturvidenskabelig uddannelse f. eks. som maskin-, bygnings- eller elektroingeniør og med minimum fem års erhvervserfaring. Det er en fordel, hvis du har erfaring fra et eller flere af følgende områder: Kalibrering, måleteknik og estimering af måleusikkerhed Laboratoriearbejde Kvalitetssikring (f. eks. inden for ISO standarder og eller andet) Auditor (intern eller ekstern) Undervisning f. eks. afholdelse af kurser Myndighedsarbejde I jobbet er der brug for at du har gode kommunikationsevner - både skriftligt og mundtligt på dansk og engelsk. Desuden forventer vi, at du har en positiv tilgang til vores kunder og overskud til at klare en til tider meget travl arbejdsdag. Om vilkårene Vi har 37 timers arbejdsuge inklusiv frokost, flekstidsordning og flere personalegoder f. eks. sundhedsforsikring og massageordning. Da rejseaktivitet er en del af jobbet, indgår dette som en del af arbejdstiden.Vil du vide mere om jobbet som ledende assessor, er du velkommen til at kontakte sektionsleder for laboratoriesektionen Kirsten M. Rosenberg (7733 9583) eller ledende assessor Erik Bruun Lorentzen (7733 9562). Ansøgning Send ansøgning med oplysning om dine kvalifikationer og din arbejdsmæssige baggrund hurtigst muligt og senest 22. september 2019 til job@danak.dk. Har du lyst til at arbejde med bedømmelse af akkrediterede laboratorier inden for kalibrering samt fysisk, mekanisk og elektrisk prøvning, og være med til at lægge grundlaget for national og international anerkendelse af laboratorier så er du måske vores nye medarbejder. DANAK er udpeget som det nationale akkrediteringsorgan i Danmark. EU-Kommissionen har anerkendt akkreditering som et centralt element i styrkelse af det Indre Marked. Læs mere om DANAK og Den Danske Akkrediteringsfond på www.danak.dk

Har du lyst til at arbejde med bedømmelse af akkrediterede laboratorier inden for kalibrering samt fysisk, mekanisk og elektrisk prøvning, og være med til at lægge grundlaget for national og international anerkendelse af laboratorier så er du måske vores nye medarbejder.

 

Som ledende assessor hos DANAK får du en uddannelse, der vil lære dig om de metoder vi bruger til bedømmelse af laboratorier og sikre dig forståelse for de akkrediteringsstandarder, som laboratorierne arbejder i henhold til. I uddannelsesforløbet vil du først være observatør på et antal bedømmelser, hvorefter du under supervision selv skal varetage bedømmelse af et antal laboratorier før du godkendes som ledende assessor. Bedømmelsesarbejdet omfatter udvælgelse og ledelse af et bedømmelseshold, som udover dig består af et antal eksperter (tekniske assessorer), oftest 1-2 men i visse tilfælde op til 4-8 eksperter. Du skal desuden koordinere og planlægge bedømmelsen og varetage afrapporteringen og den opfølgning, som ligger til grund for, at et laboratorium kan akkrediteres.

Udover bedømmelse af laboratorier vil du kunne blive inddraget i drift af infrastrukturen i DANAK, som bl.a. omfatter betjening af sektorudvalg, kontakt til myndigheder, deltagelse i internationale arbejdsgrupper og komiteer, afvikling af kurser for de akkrediterede laboratorier samt regelmæssige møder med de tekniske assessorer.

Vi kan tilbyde spændende og afvekslende arbejdsopgaver i et dynamisk miljø, med gode kollegaer og en uformel omgangstone. Du kommer til at arbejde i laboratoriesektionen både på vores kontor i Skovlunde og hos de akkrediterede laboratorier i hele landet. Da der er en vis rejseaktivitet knyttet til arbejdet med lange arbejdsdage til følge, vil du have flekstid og gode muligheder for fleksibilitet i at planlægge dit arbejde.

Om os
DANAK (Den danske Akkrediteringsfond) er en selvstændig og uafhængig fond, og er Danmarks nationale akkrediteringsorgan, som foretager akkreditering af danske virksomheder.

DANAKs mission er at sikre troværdig dokumentation for overholdelse af kravspecifikationer gennem akkreditering. Det gør vi ved at akkreditere laboratorier, certificerings- og inspektionsorganer mv. til at kalibrere, måle, certificere og foretage inspektioner efter internationale standarder. Vi har et tæt samarbejde med myndigheder i Danmark og akkrediteringsorganer i andre lande.

DANAK har 30 fastansatte medarbejdere, hvoraf 23 er ledende assessorer, samt 130 eksperter tilknyttet. DANAK har akkrediteret ca. 200 laboratorier, 40 certificeringsorganer og 50 inspektionsorganer.

Om dig
Vi forestiller os, at du er akademiker eller tilsvarende med en relevant naturvidenskabelig uddannelse f. eks. som maskin-, bygnings- eller elektroingeniør og med minimum fem års erhvervserfaring. Det er en fordel, hvis du har erfaring fra et eller flere af følgende områder:
• Kalibrering, måleteknik og estimering af måleusikkerhed
• Laboratoriearbejde
• Kvalitetssikring (f. eks. inden for ISO standarder og/eller andet)
• Auditor (intern eller ekstern)
• Undervisning f. eks. afholdelse af kurser
• Myndighedsarbejde

I jobbet er der brug for at du har gode kommunikationsevner - både skriftligt og mundtligt på dansk og engelsk. Desuden forventer vi, at du har en positiv tilgang til vores kunder og overskud til at klare en til tider meget travl arbejdsdag.

Om vilkårene
Vi har 37 timers arbejdsuge inklusiv frokost, flekstidsordning og flere personalegoder f. eks. sundhedsforsikring og massageordning. Da rejseaktivitet er en del af jobbet, indgår dette som en del af arbejdstiden.
Vil du vide mere om jobbet som ledende assessor, er du velkommen til at kontakte sektionsleder for laboratoriesektionen Kirsten M. Rosenberg (7733 9583) eller ledende assessor Erik Bruun Lorentzen (7733 9562).

Ansøgning
Send ansøgning med oplysning om dine kvalifikationer og din arbejdsmæssige baggrund hurtigst muligt og senest 22. september 2019 til job@danak.dk.

Har du lyst til at arbejde med bedømmelse af akkrediterede laboratorier inden for kalibrering samt fysisk, mekanisk og elektrisk prøvning, og være med til at lægge grundlaget for national og international anerkendelse af laboratorier så er du måske vores nye medarbejder.

DANAK er udpeget som det nationale akkrediteringsorgan i Danmark.

EU-Kommissionen har anerkendt akkreditering som et centralt element i styrkelse af det Indre Marked. Læs mere om DANAK og Den Danske Akkrediteringsfond på www.danak.dk

 

DANAK DEN DANSKE AKKREDITERINGSFONDSkovlunde2019-08-23T00:00:002019-09-22T00:00:00
330073053Senior QA Specialist, Supplier Quality ManagementRobot About Us At Radiometer, our mission is to help caregivers make diagnostic decisions that save lives. To provide caregivers the insight and confidence that help them arrive at the right diagnostic decisions decisions that in the end help save lives. On a yearly basis millions of lives are touched by the information our solutions provide and that s a fact, we take very seriously the more critical the setting, the greater the requirements are and that s why we ve made it our vision to improve global healthcare with reliable, fast and easy patient diagnoses. Want to know more about our mission and vision? Click on the link: Link of YouTube video Our people At Radiometer, we acknowledge that the information our products provide is often the difference between life and death an acknowledgement that drives and unites us as a company. From biotech and software specialists to financial controllers and engineers, all 3200 colleagues are committed and dedicated to help realize life s potential. If you aspire to be part of a purpose, performance and values driven organization whose mission and vision guide every action, we are eager to hear from you. Description We are growing and changing. So are our needs for supply. Be a dedicated QA specialist and use your experience to help us revise and implement new QMS procedures for an even better Supplier Quality Management, SQM. You will join the QA specialist team within Supplier Quality Management in Brønshøj and take part in our mission to ensure product supplies fulfil RMED specifications and quality requirements. Perform QA within SQM and develop new QA initiatives Collaborating with Global Procurement team, production, R D and many other functions in the organisation, you secure high quality and reliable products from our suppliers placed worldwide. Your mission is not only to perform QA on current suppliers, but also to partake in new supplier selection, approval, implementation and maintenance. To achieve this, you: Plan and conduct system audit of the Quality Management System and process audit of the production at the current and new suppliers in accordance with ISO 13485:2016 and MDSAP Classify suppliers to ensure right focus depending on risks, challenges and opportunities If required pre-approval of new supplier in form of e.g. a supplier visits Implement and approve Quality Agreements Follow-up on quality matters with suppliers Participate in develop new QA procedures within SQM together with the team and involved departments. The SQM area is under updating and there are great possibilities to contribute in optimizing the way of working and the QMS procedures QA supplier quality evaluation meetings Travel approximately 30-40 days per year to visit suppliers and perform audits The supplier portfolio is broad and are within outsourced processes, outsourced services, contract manufactures and critical suppliers. We offer you A unique opportunity to work in the field of medical technology, where knowledge sharing and professionalism combine to make it both fun and meaningful to go to work. Both in Denmark and abroad you will meet enthusiastic colleagues who take pride in making a difference in a company whose products can truly impact other people s lives. We offer you freedom with responsibility , opportunities for training and career development, and a wide range of staff benefits. Application deadline Application deadline is Sunday 1 September 2019. Start the application process by pressing Apply Online and follow the guidelines on our corporate career site. Please attach your CV and other relevant documents. We look forward to receiving your application. For further information, please contact Senior Recruiter, Peter Høgh, 45 61 79 55 64 or QA Specialist Liselotte Siim at 45 30 11 90 48. Qualifications Experienced QA specialist with knowledge of production and R DPassionate about quality and highly independent in your work, you are ready to take on own responsibility and make decisions that may influence the final product and potentially the lives of consumers worldwide. You also: Possess 5 years of experience with QA, reliability and SQM in the Medical Device, IVD, pharma or similar regulated industries preferably related to production, product quality and or R D Have an engineering or pharmaceutical degree Preferably, have knowledge of ISO 13485:2016, FDA QSR and MDSAP Speak and write English fluently Danaher Corporation Overview Danaher is a global science technology innovator committed to helping our customers solve complex challenges and improve quality of life worldwide. Our world class brands are leaders in some of the most demanding and attractive industries, including life sciences, medical diagnostics, dental, environmental and applied solutions. Our globally diverse team of 71,000 associates is united by a common culture and operating system, the Danaher Business System, which serves as our competitive advantage. We generated $19.9B in revenue last year. We are ranked 162 on the Fortune 500 and our stock has outperformed the S P 500 by more than 5,200 over 25 years. At Danaher, you can build a career in a way no other company can duplicate. Our brands allow us to offer dynamic careers across multiple industries. We re innovative, fast-paced, results-oriented, and we win. We need talented people to keep winning. Here you ll learn how DBS is used to shape strategy, focus execution, align our people, and create value for customers and shareholders. Come join our winning team.Danaher is committed to competitive compensation that typically has key components including base salary, variable annual incentive compensation based on personal and company performance, and long-term incentive. Organization: Radiometer Job Function: Engineering Primary Location: EMEA-Western Europe-Denmark-Hovedstaden-Brønshøj Schedule: Full-time

About Us

At Radiometer, our mission is to help caregivers make diagnostic decisions that save lives. To provide caregivers the insight and confidence that help them arrive at the right diagnostic decisions – decisions that in the end help save lives. 

On a yearly basis millions of lives are touched by the information our solutions provide and that’s a fact, we take very seriously; the more critical the setting, the greater the requirements are and that’s why we’ve made it our vision to improve global healthcare with reliable, fast and easy patient diagnoses. 

Want to know more about our mission and vision? Click on the link: Link of YouTube video 

Our people

At Radiometer, we acknowledge that the information our products provide is often the difference between life and death; an acknowledgement that drives and unites us as a company. From biotech and software specialists to financial controllers and engineers, all 3200 colleagues are committed and dedicated to help realize life’s potential.

If you aspire to be part of a purpose, performance and values driven organization whose mission and vision guide every action, we are eager to hear from you. 


Description

We are growing and changing. So are our needs for supply. Be a dedicated QA specialist and use your experience to help us revise and implement new QMS procedures for an even better Supplier Quality Management, SQM.
You will join the QA specialist team within Supplier Quality Management in Brønshøj and take part in our mission to ensure product supplies fulfil RMED specifications and quality requirements.

Perform QA within SQM and develop new QA initiatives

Collaborating with Global Procurement team, production, R&D and many other functions in the organisation, you secure high quality and reliable products from our suppliers placed worldwide. Your mission is not only to perform QA on current suppliers, but also to partake in new supplier selection, approval, implementation and maintenance. To achieve this, you:

  • Plan and conduct system audit of the Quality Management System and process audit of the production at the current and new suppliers in accordance with ISO 13485:2016 and MDSAP
  • Classify suppliers to ensure right focus depending on risks, challenges and opportunities
  • If required pre-approval of new supplier in form of e.g. a supplier visits
  • Implement and approve Quality Agreements
  • Follow-up on quality matters with suppliers
  • Participate in develop new QA procedures within SQM together with the team and involved departments. The SQM area is under updating and there are great possibilities to contribute in optimizing the way of working and the QMS procedures
  • QA supplier quality evaluation meetings
  • Travel approximately 30-40 days per year to visit suppliers and perform audits
  • The supplier portfolio is broad and are within outsourced processes, outsourced services, contract manufactures and critical suppliers.


We offer you

A unique opportunity to work in the field of medical technology, where knowledge sharing and professionalism combine to make it both fun and meaningful to go to work. Both in Denmark and abroad you will meet enthusiastic colleagues who take pride in making a difference in a company whose products can truly impact other people's lives. We offer you 'freedom with responsibility', opportunities for training and career development, and a wide range of staff benefits.

Application deadline

Application deadline is Sunday 1 September 2019. Start the application process by pressing "Apply Online" and follow the guidelines on our corporate career site. Please attach your CV and other relevant documents. We look forward to receiving your application.
For further information, please contact Senior Recruiter, Peter Høgh, +45 61 79 55 64 or QA Specialist Liselotte Siim at + 45 30 11 90 48.  

Qualifications

Experienced QA specialist with knowledge of production and R&DPassionate about quality and highly independent in your work, you are ready to take on own responsibility and make decisions that may influence the final product and potentially the lives of consumers worldwide.
You also:

  • Possess 5+ years of experience with QA, reliability and SQM in the Medical Device, IVD, pharma or similar regulated industries – preferably related to production, product quality and/ or R&D
  • Have an engineering or pharmaceutical degree
  • Preferably, have knowledge of ISO 13485:2016, FDA QSR and MDSAP
  • Speak and write English fluently

Danaher Corporation Overview

Danaher is a global science & technology innovator committed to helping our customers solve complex challenges and improve quality of life worldwide. Our world class brands are leaders in some of the most demanding and attractive industries, including life sciences, medical diagnostics, dental, environmental and applied solutions. Our globally diverse team of 71,000 associates is united by a common culture and operating system, the Danaher Business System, which serves as our competitive advantage. We generated $19.9B in revenue last year. We are ranked #162 on the Fortune 500 and our stock has outperformed the S&P 500 by more than 5,200% over 25 years.
At Danaher, you can build a career in a way no other company can duplicate. Our brands allow us to offer dynamic careers across multiple industries. We're innovative, fast-paced, results-oriented, and we win. We need talented people to keep winning. Here you'll learn how DBS is used to shape strategy, focus execution, align our people, and create value for customers and shareholders. Come join our winning team.Danaher is committed to competitive compensation that typically has key components including base salary, variable annual incentive compensation based on personal and company performance, and long-term incentive. 

Organization:  Radiometer
Job Function:  Engineering
Primary Location:  EMEA-Western Europe-Denmark-Hovedstaden-Brønshøj
Schedule:  Full-time

RADIOMETER MEDICAL ApSBrønshøj2019-08-14T00:00:002019-09-01T00:00:00
da-DK

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